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CaliberLIMS® complies with the regulations laid down by the all-important US FDA 21 CFR.

FDA 21 CFR 211.68: Deals with the Suitability & Inspection of Equipment to be used for recording the data.

FDA 21 CFR 211.160: General requirements (4): Deals with the calibration of instruments, apparatus, gauges, and recording devices.

FDA 21 CFR 820.72: Deals with documentation of procedures for utilization of the technical equipment complying with the national or international standards.

CaliberLIMS® has the built-in systems to cater to all the above requirements laid down by the US FDA.